chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105982976159829762TC29GENIChomozygous116608848
105983000859830009CT27GENIChomozygous116608850
105983016259830163GA21GENIChomozygous116608852
105983038459830385CT24GENIChomozygous116608854
105983093459830935TC30GENIChomozygous116608856
105983166859831669GC24GENIChomozygous116608858
105983174859831749GA24GENIChomozygous116608860
105983181959831820CA25GENIChomozygous116608862
105983197259831973CT21GENIChomozygous116608864
105983231259832313TC19GENIChomozygous116608866
105983267459832675GA21GENIChomozygous116608868
105983285759832858GT40GENIChomozygous116608870
105983292659832927TC25GENIChomozygous116608872
105983308759833088CT22GENIChomozygous116608874
105983439959834400GT19GENIChomozygous116608876
105983485159834852AT23GENIChomozygous116608878
105983499459834999AAACC13GENIChomozygous128820937
105983729359837294GA25GENIChomozygous116608880
105983791659837917AG32GENIChomozygous116608882
105983812759838128TA17GENIChomozygous117060976
105983812859838129TA16GENIChomozygous117060978
105983990959839910TC23GENIChomozygous116608884
105984039359840394AG21GENICpossibly homozygous116608886
105984050959840510TG19GENIChomozygous116608888
105984089359840894CT33GENICpossibly homozygous116608890
105984343959843439A15GENIChomozygous128820938
105984395659843957TC22GENIChomozygous116608898
105984267059842671TC24GENIChomozygous116608892
105984292359842924AG20GENIChomozygous116608896
105984544859845449A29GENIChomozygous128820940
105984566959845670TC13GENIChomozygous116608900
105984787659847877CT16GENIChomozygous116608902
105984844459848445CT19GENIChomozygous116608904
105985467359854674TC21GENIChomozygous116608908
105986005059860051GT17GENIChomozygous116608910
105986089459860895G25GENIChomozygous128820943